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大剂量冲击性甲泼尼龙治疗急性移植物抗宿主病

High dose bolus methylprednisolone for the treatment of acute graft versus host disease.

作者信息

Bacigalupo A, van Lint M T, Frassoni F, Podesta' M, Veneziano G, Avanzi G, Vitale V, Marmont A M

出版信息

Blut. 1983 Mar;46(3):125-32. doi: 10.1007/BF00320270.

Abstract

Nineteen patients with acute graft versus host disease (GvHD) following bone marrow transplantation (BMT) were treated with high dose bolus 6-methylprednisolone (BMPr), at the dose of 20 mg/kg/day i.v. for the first 3 days, 10 mg/kg/day i.v. for the following 4 days, and then at doses gradually tapered down to 1 mg/kg/day. All patients except one, who was given preventive BMPr 5 mg/kg/day i.v. on alternate days, were placed on preventive methotrexate therapy after BMT. Sixteen patients were grafted with an HLA matched, and three patients with an HLA mismatched marrow. Overall complete response rate in the HLA matched group was 43%, with an additional 50% showing a partial response. In the HLA mismatched group there were no responses and all three patients proved refractory to BMPr. With respect to organ involvement the complete and partial response rates were respectively 50% and 33% in the skin, 36% and 28% in the liver, 18% and 55% in the gut. Six of sixteen patients in the HLA matched group and none of the three in the HLA mismatched group are surviving. Thirteen patients died: nine patients for causes directly or indirectly related to GvHD, four of other causes (relapse, rejection, hemorrhage and idiopathic interstitial pneumonia). Side effects of BMPr consisted in hyperglicemia, and steroid associated gastritis in 2/3 of the patients, both of which responded well to conventional treatment. This study indicates that high dose BMPr is an effective form of treatment for established acute GvHD, and has no major side effects. The efficacy of BMPr is less clear in recipients of HLA mismatched grafts.

摘要

19例骨髓移植(BMT)后发生急性移植物抗宿主病(GvHD)的患者接受了大剂量冲击性6-甲基泼尼松龙(BMPr)治疗,静脉注射剂量为第1至3天20mg/kg/天,接下来4天10mg/kg/天,然后剂量逐渐减至1mg/kg/天。除1例患者在BMT后接受预防性BMPr静脉注射5mg/kg/天隔日给药外,所有患者均接受预防性甲氨蝶呤治疗。16例患者接受了HLA配型相合的骨髓移植,3例患者接受了HLA配型不相合的骨髓移植。HLA配型相合组的总体完全缓解率为43%,另有50%表现为部分缓解。在HLA配型不相合组中无缓解病例,所有3例患者对BMPr均耐药。就器官受累情况而言,皮肤的完全缓解率和部分缓解率分别为50%和33%,肝脏为36%和28%,肠道为18%和55%。HLA配型相合组的16例患者中有6例存活,HLA配型不相合组的3例患者均无存活。13例患者死亡:9例患者死于直接或间接与GvHD相关的原因,4例死于其他原因(复发、排斥、出血和特发性间质性肺炎)。BMPr的副作用包括高血糖以及2/3的患者出现类固醇相关性胃炎,两者对常规治疗反应良好。本研究表明,大剂量BMPr是治疗已确诊急性GvHD的有效方法,且无重大副作用。BMPr在HLA配型不相合移植物受者中的疗效尚不清楚。

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